Nu Colour Bioadaptive BB Plus Foundation - Light Golden

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Nu Colour Bioadaptive BB Plus Foundation - Light Golden
Generic name: TITANIUM DIOXIDE
Manufacturer: NSE Products, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: faae6f47-19f3-41cb-8e0d-388569b5c73d
SPL ID: 4c8e1026-d8e2-4ed1-890b-310106dbef4c
Version: 4
Effective date: 2026-04-07
Source export date: 2026-10-30
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:26:34

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 25 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M020	openfda.application_number
brand name		Nu Colour Bioadaptive BB Plus Foundation - Light Golden	openfda.brand_name
brand name		Nu Colour Bioadaptive BB Plus Foundation - Linen	openfda.brand_name
brand name		Nu Colour Bioadaptive BB Plus Foundation - Ivory	openfda.brand_name
brand name		Nu Colour Bioadaptive BB Plus Foundation - Natural Beige	openfda.brand_name
generic name		TITANIUM DIOXIDE	openfda.generic_name
manufacturer name		NSE Products, Inc.	openfda.manufacturer_name
ndc	package	62839-3362-1	openfda.package_ndc
ndc	package	62839-3365-1	openfda.package_ndc
ndc	package	62839-3364-1	openfda.package_ndc
ndc	package	62839-3363-1	openfda.package_ndc
ndc	package	62839-3361-1	openfda.package_ndc
ndc	product	62839-3364	openfda.product_ndc
ndc	product	62839-3361	openfda.product_ndc
ndc	product	62839-3365	openfda.product_ndc
ndc	product	62839-3363	openfda.product_ndc
ndc	product	62839-3362	openfda.product_ndc
ndc11	package	62839336501	derived:openfda.package_ndc
ndc11	package	62839336101	derived:openfda.package_ndc
ndc11	package	62839336301	derived:openfda.package_ndc
ndc11	package	62839336201	derived:openfda.package_ndc
ndc11	package	62839336401	derived:openfda.package_ndc
spl id		4c8e1026-d8e2-4ed1-890b-310106dbef4c	id
spl set id		faae6f47-19f3-41cb-8e0d-388569b5c73d	set_id
unii		15FIX9V2JP	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use on damaged or broken skin. Stop use and ask a doctor if a rash occurs. When using this product, keep out of eyes. Rinse with water to remove. Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.